Formaldehyde-free binder compositions and methods of making the binders under controlled acidic conditions

ABSTRACT

Formaldehyde-free binder compositions are described that include an aldehyde or ketone, a reaction product between a polyamine and an organic anhydride, and an acidic compound. The acidic compound may be an organic acid, an acidic catalyst, or both. The acidic compound is supplied in quantities that lower the pH of the binder composition to about 5 or less. The binder compositions may be used in methods of binding fiberglass and the resulting fiberglass products have an improved tensile strength due to the addition of the acidic compound.

CROSS-REFERENCES TO RELATED APPLICATIONS

This application is a continuation of Applicant's pending U.S.Non-Provisional patent application Ser. No. 13/478,765 filed May 23,2012, which is a continuation-in-part of Applicant's U.S. applicationSer. No. 12/539,263 filed Aug. 11, 2009, now U.S. Pat. No. 9,365,963issued Jun. 14, 2016. This application is also related to Applicant'sU.S. application Ser. No. 12/539,211, now abandoned; Ser. No. 12/543,607filed Aug. 19, 2009, now U.S. Pat. No. 8,708,162 issued Apr. 29, 2014;Ser. No. 12/543,586 filed Aug. 19, 2009, now U.S. Pat. No. 8,651,285issued Feb. 18, 2014; Ser. No. 12/543,625 filed Aug. 18, 2009, now U.S.Pat. No. 8,372,900 issued Feb. 12, 2013; Ser. No. 12/543,574 filed Aug.19, 2009, now U.S. Pat. No. 8,377,564 issued Feb. 19, 2013; Ser. No.12/633,828 filed Dec. 9, 2009, now abandoned; Ser. No. 13/386,843 filedMar. 6, 2012, now U.S. Pat. No. 8,940,854 issued Jan. 27, 2015; andpending Ser. No. 13/386,865 filed Mar. 6, 2012. The entire contents ofthe above-listed applications are herein incorporated by reference forall purposes.

BACKGROUND OF THE INVENTION

The subject invention pertains to an improved binding composition foruse with fiberglass. More specifically, the invention pertains to animproved curable composition comprising an addition product of an amineand a reactant in the form of an amino-amide intermediate. An aldehydeor ketone is added to the amino-amide to form a composition which uponcuring is capable of forming a water-insoluble polymer composition whichdisplays good adhesion to glass. Once applied to the fiberglass, thebinding composition is cured. The binder of the present invention isuseful as a fully acceptable replacement for formaldehyde-based bindersin non-woven fiberglass products, and actually provides a binderexhibiting improved physical properties.

Fiberglass binders have a variety of uses ranging from stiffeningapplications where the binder is applied to woven or non-wovenfiberglass sheet goods and cured, producing a stiffer product;thermo-forming applications wherein the binder resin is applied to asheet or lofty fibrous product, following which it is dried andoptionally B-staged to form an intermediate but yet curable product; andto fully cured systems such as building insulation.

Fibrous glass insulation products generally comprise matted glass fibersbonded together by a cured thermoset polymeric material. Molten streamsof glass are drawn into fibers of random lengths and blown into aforming chamber where they are randomly deposited as a mat onto atraveling conveyor. The fibers, while in transit in the forming chamberand while still hot from the drawing operation, are sprayed with anaqueous binder. A phenol-formaldehyde binder has been used throughoutthe fibrous glass insulation industry. The residual heat from the glassfibers and the flow of air through the fibrous mat during the formingoperation are generally sufficient to volatilize water from the binder,thereby leaving the remaining components of the binder on the fibers asa viscous or semi-viscous high solid liquid. The coated fibrous mat istransferred to a curing oven where heated air, for example, is blownthrough the mat to cure the binder and rigidly bond the glass fiberstogether.

Fiberglass binders used in the present sense should not be confused withmatrix resins which are an entirely different and non-analogous field ofart. While sometimes termed “binders”, matrix resins act to fill theentire interstitial space between fibers, resulting in a dense, fiberreinforced product where the matrix must translate the fiber strengthproperties to the composite, whereas “binder resins” as used herein arenot space-filling, but rather coat only the fibers, and particularly thejunctions of fibers. Fiberglass binders also cannot be equated withpaper or wood product “binders” where the adhesive properties aretailored to the chemical nature of the cellulosic substrates. Many suchresins are not suitable for use as fiberglass binders. One skilled inthe art of fiberglass binders would not look to cellulosic binders tosolve any of the known problems associated with fiberglass binders.

Binders useful in fiberglass insulation products generally require a lowviscosity in the uncured state, yet possess characteristics so as toform a rigid thermoset polymeric binder for the glass fibers when cured.A low binder viscosity in the uncured state is required to allow the matto be sized correctly. Also, viscous binders commonly tend to be tackyor sticky and hence they lead to the accumulation of fiber on theforming chamber walls. This accumulated fiber may later fall onto themat causing dense areas and product problems. A binder which forms arigid matrix when cured is required so that a finished fiberglassthermal insulation product, when compressed for packaging and shipping,will recover to its as-made vertical dimension when installed in abuilding.

From among the many thermosetting polymers, numerous candidates forsuitable thermosetting fiberglass binder resins exist. However,binder-coated fiberglass products are often of the commodity type, andthus cost becomes a driving factor, generally ruling out resins such asthermosetting polyurethanes, epoxies, and others. Due to their excellentcost/performance ratio, the resins of choice in the past have beenphenol-formaldehyde resins. Phenol-formaldehyde resins can beeconomically produced, and can be extended with urea prior to use as abinder in many applications. Such urea-extended phenol-formaldehydebinders have been the mainstay of the fiberglass insulation industry foryears, for example.

Over the past several decades however, minimization of volatile organiccompound emissions (VOCs) and hazardous air pollutants (HAPS) both onthe part of the industry desiring to provide a cleaner environment, aswell as by Federal regulation, has led to extensive investigations intonot only reducing emissions from the current formaldehyde-based binders,but also into candidate replacement binders. For example, subtle changesin the ratios of phenol to formaldehyde in the preparation of the basicphenol-formaldehyde resole resins, changes in catalysts, and addition ofdifferent and multiple formaldehyde scavengers, has resulted inconsiderable improvement in emissions from phenol-formaldehyde bindersas compared with the binders previously used. However, with increasinglystringent Federal regulations, more and more attention has been paid toalternative binder systems which are free from formaldehyde.

One such candidate binder system employs polymers of acrylic acid as afirst component, and a polyol such as triethanolamine, glycerine, or amodestly oxyalkylated glycerin as a curing or “crosslinking” component.The preparation and properties of such poly(acrylic acid)-based binders,including information relative to the VOC emissions, and a comparison ofbinder properties versus urea-formaldehyde binders is presented in“Formaldehyde-Free Crosslinking Binders For Non-Wovens,” Charles T.Arkins et al., TAPPI Journal, Vol. 78, No. 11, pages 161-168, November1995. The binders disclosed by the Arkins article, appear to beB-stageable as well as being able to provide physical properties similarto those of urea/formaldehyde resins.

U.S. Pat. No. 5,340,868 discloses fiberglass insulation products curedwith a combination of a polycarboxy polymer, a-hydroxyalkylamide, and atleast one trifunctional monomeric carboxylic acid such as citric acid.The specific polycarboxy polymers disclosed are poly(acrylic acid)polymers. See also, U.S. Pat. No. 5,143,582.

U.S. Pat. No. 5,318,990 discloses a fibrous glass binder which comprisesa polycarboxy polymer, a monomeric trihydric alcohol and a catalystcomprising an alkali metal salt of a phosphorous-containing organicacid.

U.S. 2007/0142596 discloses binders comprised of a mixture of Maillardreactants. The reactants comprise a monosaccharide and an ammonium saltof a polycarboxylic acid.

Published European Patent Application EP 0 583 086 A1 appears to providedetails of polyacrylic acid binders whose cure is catalyzed by aphosphorus-containing catalyst system as discussed in the Arkins articlepreviously cited. Higher molecular weight poly(acrylic acids) are statedto provide polymers exhibiting more complete cure. See also U.S. Pat.Nos. 5,661,213; 5,427,587; 6,136,916; and 6,221,973.

Some polycarboxylic polymers have been found useful for makingfiberglass insulation products. Problems of clumping or sticking of theglass fibers to the inside of the forming chambers during theprocessing, as well as providing a final product that exhibits therecovery and rigidity necessary to provide a commercially acceptablefiberglass insulation product, have been overcome. See, for example,U.S. Pat. No. 6,331,350. The thermosetting acrylic resins have beenfound to be more hydrophilic than the traditional phenolic binders,however. This hydrophilicity can result in fiberglass insulation that ismore prone to absorb liquid water, thereby possibly compromising theintegrity of the product. Also, the thermosetting acrylic resins nowbeing used as binding agents for fiberglass have been found to not reactas effectively with silane coupling agents of the type traditionallyused by the industry increasing product cost. The addition of siliconeas a hydrophobing agent results in problems when abatement devices areused that are based on incineration as well as additional cost. Also,the presence of silicone in the manufacturing process can interfere withthe adhesion of certain facing substrates to the finished fiberglassmaterial. Overcoming these problems will help to better utilizepolycarboxylic polymers in fiberglass binders.

Accordingly, in one aspect the present invention provides a novel,non-phenol-formaldehyde binder.

Another aspect of the invention provides a novel fiberglass binder whichprovides advantageous flow properties, the possibility of lower binderusage, the possibility of overall lower energy consumption, eliminationof interference in the process by a silicone, and improved overalleconomics.

Still another aspect of the present invention is to provide a binder forfiberglass having improved economics, while also enjoying improvedphysical properties. In addition, the present invention increases thesustainable portion of the binder and reduces the dependency on a fossilbased source for the resin.

These and other aspects of the present invention will become apparent tothe skilled artisan upon a review of the following description and theclaims appended hereto.

BRIEF SUMMARY OF THE INVENTION

A curable composition for use in the binding of fiberglass is providedcomprising an addition product of an amine and a saturated orunsaturated reactant in the form of an amino-amide intermediate. To thisintermediate is added an aldehyde or ketone, preferably a reducingsugar, to form a curable binder composition. This composition uponcuring is capable of forming a water-insoluble polymer composition whichexhibits good adhesion to glass.

Additional examples of the present curable, formaldehyde-free bindercompositions include compositions having an aldehyde or ketone, areaction product between a polyamine and an organic anhydride, and anacidic compound. The acidic compound may be an organic acid, an acidiccatalyst, or both. The acidic compound is supplied in quantities thatlower the pH of the binder composition to about 5 or less. When thebinder compositions are heat cured, the aldehyde or ketone react withthe reaction product to form the polymerized binder.

A process for binding fiberglass is provided comprising applying tofiberglass a coating of a composition comprising an addition product ofan amine and a saturated or unsaturated reactant in the form of anamino-amide intermediate, to which is added an aldehyde or ketone.Thereafter the composition is cured while present as a coating on thefiberglass to form a water-insoluble polymer composition which exhibitsgood adhesion to the fiberglass.

In one embodiment, the reaction product of a polyamine and an organicanhydride may be the amino-amide intermediate. The intermediate mayundergo heating to create an amino-amide oligomer before beingintroduced to the aldehyde or ketone. The aldehyde or ketone and theacidic compound are then added to the amino-amide oligomer, and theresulting binder composition is applied to fiberglass and cured to makea fiberglass product.

In a preferred embodiment the resulting fiberglass product is buildinginsulation. A roofing membrane is also a useful application. In otherembodiments the fiberglass product is a microglass-based substrateuseful when forming a printed circuit board, battery separator, filterstock, or reinforcement scrim.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a graph showing tensile strength performance for a group ofglass composites;

FIG. 2 is a graph showing tensile strength performance for another groupof glass composites; and

FIG. 3 is a picture of a cured dogbone composite placed in an Instrontensile strength measuring instrument.

DETAILED DESCRIPTION OF THE INVENTION

The novel fiberglass binder composition of the present invention is acurable composition comprising the reaction product of an amine and asaturated or unsaturated reactant to form an amino-amide intermediate.

In accordance with one embodiment of the invention, amine reactants areselected which are capable of undergoing conjugate addition to form therequisite amino-amide, which forms a water-insoluble polyimide uponcuring. In such an embodiment the amine is a di- or multi-functionalprimary or secondary amine. More preferably, the amine is a diaminehaving at least one primary amine group.

Example of amines include, but are not limited to, aliphatic,cycloaliphatic and aromatic amines. The amines may be linear orbranched. The amine functionalities may be di- or multifunctionalprimary or secondary amines. The amines can include otherfunctionalities and linkages such as alcohols, thiols, esters, amides,acids, ethers and others.

Representative amines that are suitable for use in such an embodimentinclude 1,2-diethylamine, 1,3-propanediamine, 1,4-butanediamine,1,5-pentanediamine, 1,6-hexanediamine, .alpha.,.alpha.′-diaminoxylene,diethylenetriamine, triethylenetetramine, tetraethylenepentamine, andmixtures of these. Preferred diamines for use in this embodiment of theinvention are 1,4-butanediamine and 1,6-hexanediamine. Natural andsynthetic amino acids such as lysine, anginine, hestidine, etc. can alsobe used.

The curable amino-amide is formed through the selection of anunsaturated or saturated reactant that is an anhydride, carboxylic acid,ester, and salts and mixtures of such reactants. Representativeunsaturated reactants are maleic acid, fumaric acid, maleic anhydride,mono- and di-esters of maleic acid and fumaric acid, and salts andmixtures of these. Ammonium salts of the unsaturated acids of theirmonoesters conveniently can be utilized. A preferred unsaturatedreactant is maleic anhydride. Representative saturated reactantsinclude, but are not limited to, succinic anhydride, succinic acid, monoand diesters of succinic acid, glutaric acid and anhydride, phthalicacid and anhydride, tetrahydro phthaic acid and anhydride, mono anddiesters of acid anhydrides and salts of the acids, and their monoesters. A preferred saturated reactant is phthalic anhydride ortetrahydro phthalic anhydride.

The amino-amide addition products can be readily formed by mixing thecomponents in an aqueous medium at room temperature. The resultingaddition products are either water-soluble, water-dispersible, or arepresent as an emulsion. To the solution of amino-amide, the carbonylfunctional materials can be added, especially an aldehyde or ketone. Dueto their higher reactivity, aldehydes are preferred to ketones. Thecomposition comprises the amino-amide and the aldehyde and/or ketone.Some reaction does take place within the composition between thecomponents. However, the reaction is completed during the curing step,followed by the cross-linking reaction of curing.

Examples of suitable aldehydes include, but are not limited to, mono-and multifunctional aldehydes including acetaldehyde, hydroxyacetaldehyde, butyraldehyde, acrolein, furfural, glyoxal,glyceraldehyde, glutaraldehyde, polyfurfural, polyacrolein, copolymersof acrolein and others. Reducing mono, di- and polysaccharides such asglucose, maltose, etc. can be used, with reducing monosaccharides suchas glucose being preferred.

Examples of ketones include, but are not limited to, acetone, acetylacetone, 1,3-dihydroxy acetone, benzyl, benzoin, fructose, etc.

The aldehydes and ketones react with the amino-amide intermediate, whichcontains an amic acid function, i.e., an amide linkage in the vicinityof a carboxylic acid. An amic acid function is more reactive than asimple carboxylic acid. The amount of aldehyde and/or ketone added isgenerally such that the molar ratio of carboxylic acid in theamino-amide to carbonyl or ketone is from 1:5 to 50:1. A ratio of 1:20to 20:1 is more preferred, with a ratio of 1:10 to 10:1 being mostpreferred.

One advantage is that the presence of all functional groups, i.e.,amine, amide and carboxylic acid, on the same molecule eliminates thepotential need for the addition of external crosslinkers or binders suchas polycarboxylic acids and/or polyvinyl alcohol. Such crosslinkers canbe added, however if desired.

In an embodiment, the amino-amide can be first oligomerized prior toadding the aldehyde or ketone. The amino-amide can be heated until anoligomer is obtained, e.g., a dimer, trimer or tetramer of theamino-amide intermediate. An example of suitable conditions for makingthe oligomer involves heating in the range of from 120-150° C. for up to5 hours.

Using the oligomerized product has been found to result in a more robustbinder product upon curing. This manifests itself in the strength of thebinder, and allows for better storage results, higher tensile strengthand rigidity, and better recovery for products made with the binder.

The composition when applied to the fiberglass optionally can includeadhesion prompters, oxygen scavengers, solvents, emulsifiers, pigments,fillers, anti-migration aids, coalescent aids, wetting agents, biocides,plasticizers, organosilanes, anti-foaming agents, colorants, waxes,suspending agents, anti-oxidants, crosslinking catalysts, secondarycrosslinkers, and combinations of these.

The binder composition may also include acids and/or acidic catalyststhat lower the overall pH of the binder. Exemplary acids include organicacids that have one or more carboxylic acid groups. For example, theorganic acid may be a monocarboxylic acid such as a C₁-C₁₂ carboxylicacid (e.g., acetic acid), or an aromatic carboxylic acid (e.g., benzoicacid), among others. Exemplary organic acids may also includedicarboxylic acids such aliphatic dicarboxylic acids, unsaturated (e.g.,olefinic) dicarboxylic acids, and aromatic dicarboxylic acids, amongothers. Exemplary aliphatic dicarboxylic acids may include oxalic acid,malonic acid, succinic acid, glutaric acid, adipic acid, pimelic acid,suberic acid, azelaic acid, sebacic acid, undecanedioic acid, anddodecanedioic acid, among others. Exemplary olefinic dicarboxylic acidsmay include maleic acid, fumaric acid, glutaconic acid, traumatic acid,itaconic acid, and muconic acid among others. Exemplary aromaticdicarboxylic acids may include phthalic acid, isophthalic acid, andterephthalic acid, among others. Exemplary organic acids may alsoinclude tricarboxylic acids such as citric acid, isocitric acid,aconitic acid, propane-1,2,3-tricarboxylic acid, and trimesic acid,among others. Still further examples of organic acids may includepolycarboxylic acids having two or more carboxylic acid groups, such asmellitic acid, tartaric acid, etc.

Exemplary acidic catalysts include salts of sulfuric (H₂SO₄), phosphoric(H₃PO₄), or nitric acid (HNO₃). These include ammonium salts of theacids, where one or more hydrogen ions supplied by the acid aresubstituted with an ammonium cation (NH₄ ⁺). Exemplary ammonium saltacidic catalysts include mono-ammonium sulfate (NH₄)HSO₄, di-ammoniumsulfate (NH₄)₂SO₄, mono-ammonium phosphate (NH₄)H₂PO₄, and di-ammoniumphosphate (NH₄)₂HPO₄, among others.

The fiberglass to which the composition according to the presentinvention is applied may take a variety of forms and in a preferredembodiment is building insulation. Roofing membranes is also a usefulapplication due to good characteristics. In other embodiments thefiberglass is a microglass-based substrate useful in applications suchas printed circuit boards, battery separators, filter stock, andreinforcement scrim.

The composition of the present invention can be applied to thefiberglass by a variety of techniques. In preferred embodiments theseinclude spraying, spin-curtain coating, and dipping-roll coating. Thecomposition can be applied to freshly-formed fiberglass, or to thefiberglass following collection. Water or other solvents can be removedby heating.

Thereafter the composition undergoes curing wherein a polymeric coatingis formed which exhibits good adhesion to glass. The polymericcomposition obtained upon curing is a combination of a polyamino-amideand a polyamino-imide. The polyimide is the primary product, but some ofthe amide in the intermediate is believed to not form the imide. Thus,some polyamino-amide is also present in the cured composition/binder.

Such curing can be conducted by heating. Elevated curing temperatures onthe order of 100 to 300° C. generally are acceptable. Satisfactorycuring results are achieved by heating in an air oven at 200° C. forapproximately 20 minutes.

The cured binder at the conclusion of the curing step commonly ispresent as a secure coating on the fiberglass in a concentration ofapproximately 0.5 to 50 percent by weight of the fiberglass, and mostpreferably in a concentration of approximately 1 to 10 percent by weightof the fiberglass.

The present invention provides a formaldehyde-free route to form asecurely bound formaldehyde-free fiberglass product. The bindercomposition of the present invention provides advantageous flowproperties, the elimination of required pH modifiers such as sulfuricacid and caustic, and improved overall economics and safety. The binderalso has the advantages of being stronger and offering lower amounts ofrelative volatile organic content during curing, which ensures a saferwork place and environment. The cure time of the binder is also seen tobe much faster and therefore does favor the economics, while reducingthe energy consumption during the curing process and lowering the carbonfootprint. The binder also contains a high level of sustainable rawmaterials further reducing the dependency on fossil based sources forthe resin. Also, due to the hydrophobic nature of the binder, the needfor a water repellant such as silicones is eliminated or greatlyreduced.

The following examples are presented to provide specific examples of thepresent invention. In each instance the thin glass plate substrate thatreceives the coating can be replaced by fiberglass. It should beunderstood, however, that the invention is not limited to the specificdetails set forth in the Examples.

EXAMPLES Preparation of Intermediates

To 116 g 1, 6 diaminohexane (HMDA) dissolved in 214 g water, 98 g maleicanhydride (MAn) was added slowly (molar ratio of 1:1) and the solutionwas stirred for 10 min. The intermediate was labeled HM.

To 116 g HMDA dissolved in 264 g water was added to 148 g phthalicanhydride. After the anhydride dissolved, the intermediate was labeledHP.

To 116 g HMDA dissolved in 268 g water was added 152 g tetrahydrophthalic anhydride. The solution was stirred until all anhydridedissolved. The intermediate was labeled HT.

These intermediates were utilized to make the following resins withglucose.

Example 1

To 42.8 g of solution of the HM intermediate anhydrous dextrose(alpha-D-glucose) and water were added. The mass of added water waschosen to be equal to that of the corresponding dextrose. The mass ofdextrose (and corresponding water) was 18 g, 36 g, 54 g, 72 g 90 g, 108,144, 180 g and 216 g. The various solutions were stirred at ambienttemperature for 10 mn. The solutions were applied as a thin film onglass and A1 panel, dried in an oven at 100° C. for 5 min and cured at200° C. for 20 min. Each of the solutions formed a cured brown polymerwhich was hard and insoluble in water and solvents, and showed anexcellent adhesion to glass.

Example 2

To 52.8 g of solution of the HP intermediate, anhydrous dextrose(alpha-D-glucose) and water were added. The mass of added water waschosen to be equal to that of the corresponding dextrose. The mass ofdextrose (and corresponding water) was 18 g, 36 g, 54 g, 72 g, 90 g,108, 144, 180 g and 216 g. The various solutions were stirred at ambienttemperature for 10 min. The solutions were applied as a thin film on aglass and A1 panel, dried in an oven at 100° C. for 5 min and cured at200° C. for 20 min. Each solution formed a cured brown polymer which washard and insoluble in water and solvents, and showed an excellentadhesion to glass.

Example 3

To 53.6 g of solution of the HT intermediate, anhydrous dextrose(alpha-D-glucose) and water were added. The mass of added water waschosen to be equal to that of corresponding dextrose. The mass ofdextrose (and corresponding water) was 18 g, 36 g, 54 g, 72 g, 90 g,108, 144, 180 g and 216 g. The various solutions were stirred at ambienttemperature for 10 min. The solutions were applied as a thin film onglass and A1 panel, dried in an oven at 100° C. for 5 min and cured at200° C. for 20 min. Each solution formed a cured brown polymer which washard and insoluble in water and solvents, and showed an excellentadhesion to glass.

Example 4

Examples 1-3 were repeated in the presence of 5% by weight ammoniumsulfate. The polymers became insoluble in water in less than 10 min.

Example 5

To 116 g HMDA dissolved in 214 g water was added slowly 98 g maleicanhydride (Man), this was a molar ratio of 1:1. The resulting solutionwas refluxed for 60 minutes to prepare an amino-amide oligomer. Thesolution was opaque with 50% solids. The solution was then used torepeat example 1 with the observed results being the same, i.e., thecured polymer was hard and insoluble in water and solvents, and showedexcellent adhesion to glass.

Example 6 —Plant Trial

To examine the performance of the binder on an insulation batt, a bindersolution was prepared and applied in the manufacture of the insulationbatt. Processing and performance of the batts made with the binder ofthis invention was compared with the batts manufactured with apolyacrylic acid binder cured with triethanol amine.

To prepare the binder, 116 g HMDA was dissolved in 754 kg water. To thissolution was added 98 kg maleic anhydride with stirring until dissolved.To this solution was added 540 kg anhydrous dextrose. When the dextrosedissolved, 37.7 kg ammonium sulfate was added. After all the ingredientsdissolved, the clear binder solution was utilized in the manufacture ofR-19 and R-13 insulation batt.

The binder was applied at the rate of 4.5% binder on glass fibercontaining 1% (based on binder) of an amino-propyl silane coupling agentand about 0.5% dedusting oil. The batt was cured at 210° C. with an ovenresidence time of two minutes. The 32″ droop (sag) and recovery data forR-19 insulation batt products are presented in Table 1 and Table 2 belowrespectively:

TABLE 1 32″ Droop Data for R-19 Unaged 7 Day 14 Day Control (Acrylic)1.1 1.7 2.2 HP 1.0 1.3 1.6

TABLE 2 Recovery fir R-19 Unaged 7 Day 14 Day Control (Acrylic) 6.916.48 6.38 HP 6.85 6.55 6.41

As seen from Table 1 and Table 2, the R-19 insulation product of the newformaldehyde free binder of this invention (HP) has better performancecompared to the commercial acrylic control.

Addition of Organic Acids to Binder Compositions

Another set of experiments was performed to measure the effect of thebinder's pH on the tensile strength of glass composites made with thebinder. Binder compositions were made from a combination of (i) 1,6hexanediamine (H), maleic anhydride (M), and dextrose (D) (“HMD”), with(ii) either maleic acid or citric acid. Comparative binder compositionsof HMD without added acid were also made and tested.

The HMD component of the binder compositions had a mole ratio of 1,6hexanediamine:maleic anhydride:dextrose of either 1:1:3 or 1:1:6. Themaleic or citric acid was added to the HMD component in a 1:1 moleratio. Table 3 below describes the compositions and pHs of six bindercompositions used in the tensile strength tests that were graphed inFIG. 1:

TABLE 3 Compositions and pH of HMD Binders: Entry Mole Ratio HMD OrganicAcid Moles of Acid pH 1 1:1:6 None 0 6.5 2 1:1:6 Maleic Acid 1 3.0 31:1:6 Citric Acid 1 3.2 4 1:1:3 None 0 7.2 5 1:1:3 Maleic Acid 1 3.3 61:1:3 Citric Acid 1 3.4

As shown in Table 3, the pH of the comparative binder compositions withno added acid were very slightly acidic to alkaline, while thecompositions with added maleic or citiric acid showed a drop in pH to arange from 3.0 to 3.4.

Each of the binder compositions was formulated into 25 g samples havinga 50 wt. % solids level and mixed with 1000 g of glass beads to makeuncured composites.

Roughly 1 ounce samples of the uncured composites were then spread intodogbone molds and pressed in the molds at a pressure of about 10,000lbs. The dogbone samples were then released from the molds and heated atabout 400° F. for about 20 minutes to form cured dogbone composites. Thecured dogbone composites were roughly 25 mm wide and 6 mm thick.

The cured dogbone composites were tested for tensile strength in both anunaged condition and after being aged in a high humidity atmosphere. Theunaged composites were taken directly from the curing oven and placed inan Instron tensile strength testing instrument (Harry W. DietertCo.—Tensile Core Grip Assembly Part No. 610-7CA) as shown in FIG. 3. Theaged composites were taken from the curing oven and placed for 24 hoursin a humidifying oven set at approximately 95% humidity and 120° F.After the aged samples were cooled for approximately 8 hours, they wereplaced in the Instron instrument to test their tensile strength.

FIG. 1 shows the results of the strength tests for dogbone compositesmade with the binder compositions 1-6 listed in Table 3. The results inFIG. 1 show significant improvement in the tensile strength of thedogbone composites made with the acidified binder compositions.Acidified HMD binder compositions having a 1:1:6 mole ratio of H:M:Dshowed an approximately 26% increase in tensile strength compared to the1:1:6 HMD binder composition with no added organic acid. Acidified HMDbinder compositions having a 1:1:3 mole ratio of H:M:D showed evenlarger increases in tensile strength (about 35-45% higher) than thecomparative unacidified 1:1:3 HMD binder composition. For both HMDbinder compositions, the acidification of the binder with an organicacid provided a significant increase in composite's tensile strengthcompared to the unacidified binder compositions.

Addition of Acidic Catalysts to Binder Compositions

Another set of experiments were conducted to determine whetherdecreasing binder pH using acidic catalysts made from inorganic ammoniumsulfates and phosphates could also increase the tensile strength ofglass-containing composites made with the binder compositions. In thisset of experiments catalysts were added to a binder compositions of 1,6hexanediamine (H), maleic anhydride (M), and dextrose (D) having a moleratio of 1,6 hexanediamine:maleic anhydride:dextrose of 1:1:6. Table 4below describes the four binder-catalyst compositions used in thetensile strength tests graphed in FIG. 2:

TABLE 4 Compositions and pH of HMD/Catalyst Binders: Catalyst (wt. % ofBinder Entry Mole Ratio H:M:D Composition) pH 1 1:1:6 5% (NH₄)₂SO₄ 6.5 21:1:6 5% (NH₄)HSO₄ 4.5 3 1:1:6  5% (NH₄)H₂PO₄ 6.0 4 1:1:6 10% (NH₄)H₂PO₄5.2

Binder compositions 1-4 were each mixed with glass beads to form uncuredcomposites that were then molded, pressed, and heat cured into dogbonecomposites as described in the organic acid addition tests above. Thedogbone composites were they placed in the Instron tensile strengthtesting instrument and the tensile strength test results were recordedand graphed in FIG. 2. As FIG. 2 shows, the addition of the more acidicmono-ammonium sulfate to the binder produced a dogbone composite withsignificantly higher tensile strength than the more alkaline di-ammoniumsulfate catalyst. Improved tensile strength of unaged dogbone compositeswas also observed when the amount of mono-ammonium phosphate was doubledfrom 5% to 10%, resulting a drop in the binder composition pH from 6.0to 5.2.

The experimental results of adding an organic acid (e.g., maleic acid,citric acid) or an acidic catalyst (e.g., acidic ammonium sulfate andphosphate salts) show that the addition of these compounds in amountsthat reduce the binder composition's pH below 5.0 can significantlyincrease the tensile strength of glass-fiber composites made with theacidified binders. A reduction in the alkalinity of the bindercompositions may also increase their tensile strength at pHs above 5.0,although the magnitude of the increase may not be as large.

The principles, preferred embodiments, and modes of operation of thepresent invention have been described in the foregoing specification.The invention which is intended to be protected herein, however, is notto be construed as limited to the particular forms disclosed, sincethese are to be regarded as illustrative rather than restrictive.Variations and changes may be made by those skilled in the art withoutdeparting from the spirit of the invention.

What is claimed is:
 1. A method of making a fiberglass product, themethod comprising: combining a binder composition and glass fibers,wherein the binder composition includes: an aldehyde or ketone, anamino-amide compound, and a catalyst for catalyzing a reaction between(i) the aldehyde or ketone and (ii) the amino-amide compound; formingthe combination of the binder composition and the glass fibers into anuncured fiberglass mat or batt; and heating the uncured fiberglass mator batt into the fiberglass product.
 2. The method of claim 1, whereinthe aldehyde or ketone comprises a reducing sugar.
 3. The method ofclaim 2, wherein the reducing sugar comprises dextrose.
 4. The method ofclaim 1, wherein the amino-amide compound is an amino-amide oligomer. 5.The method of claim 1, wherein the amino-amide compound is a reactionproduct of an amine and a carbonyl compound.
 6. The method of claim 5,wherein the amine comprises at least one of 1,2-diethylamine,1,3-propanediamine, 1,4-butanediamine, 1,5-pentanediamine,1,6-hexanediamine, α, α′-diaminoxylene, diethylenetriamine,triethylenetetramine, or tetraethylenepentamine.
 7. The method of claim5, wherein the amine comprises an amino acid.
 8. The method of claim 5,wherein the carbonyl compound comprises at least one of an organic acidanhydride, a carboxylic acid, an organic ester, or a salt thereof. 9.The method of claim 8, wherein the carboxylic acid comprises at leastone of maleic acid, fumaric acid, succinic acid, glutaric acid, phthalicacid, or tetrahydrophthaic acid.
 10. The method of claim 8, wherein theorganic acid anhydride comprises at least one of maleic anhydride,succinic anhydride, glutaric anhydride, phthalic anhydride, ortetrahydrophthaic anhydride.
 11. The method of claim 5, wherein thecarbonyl compound comprises an ammonium salt of a carboxylic acid ororganic acid anhydride.
 12. The method of claim 1, wherein the catalystis an acidic compound that sets a pH for the binder composition to 5 orless.
 13. The method of claim 12, wherein the acidic compound comprisesan organic acid or an inorganic acid.
 14. The method of claim 13,wherein the organic acid comprises a polycarboxylic acid.
 15. The methodof claim 14, wherein the polycarboxylic acid comprises citric acid. 16.The method of claim 13, wherein the inorganic acid comprises at leastone of sulfuric acid, phosphoric acid, nitric acid or ammonium saltsthereof.
 17. The method of claim 1, wherein the binder composition iscombined with the glass fibers before they are collected and formed intothe uncured fiberglass mat or batt.
 18. The method of claim 1, whereinthe uncured fiberglass mat or batt is heated at 100° C. to 300° C. 19.The method of claim 1, wherein the fiberglass product comprisesfiberglass insulation.
 20. A method of making fiberglass insulation, themethod comprising: providing glass fibers; applying a binder compositionto the glass fibers, wherein the binder composition comprises (i) apolysaccharide, (ii) an ammonium salt, and (iii) a polycarboxylic acid;forming the glass fibers having the applied binder composition into anuncured fiberglass batt; and heating the uncured fiberglass batt intothe fiberglass insulation.
 21. The method of claim 20, wherein thepolycarboxylic acid comprises a dicarboxylic acid or a tricarboxylicacid.
 22. The method of claim 21, wherein the dicarboxylic acidcomprises itaconic acid.
 23. The method of claim 21, wherein thetricarboxylic acid comprises citric acid.
 24. The method of claim 21,wherein the binder composition has a pH of 5 or less.
 25. A method ofmaking fiberglass insulation, the method comprising: providing glassfibers; applying a binder composition to the glass fibers, wherein thebinder composition comprises (i) dextrose, (ii) a multifunctionalaldehyde, and (iii) an inorganic acid; forming the glass fibers havingthe applied binder composition into an uncured fiberglass batt; andheating the uncured fiberglass batt into the fiberglass insulation. 26.The method of claim 25, wherein the multifunctional aldehyde comprisesglyoxal.
 27. The method of claim 25, wherein the inorganic acidcomprises sulfuric acid.
 28. The method of claim 25, wherein the bindercomposition has a pH of 5 or less.